Genetic Disorders

Body Morphology, Thanatophoric Dysplasia Type II

Body Morphology, Thanatophoric Dysplasia Type II

Brain, Thanatophoric Dysplasia Type II

Peripheral Blood, Sickle cell anemia

Skeleton, Thanatophoric Dysplasia Type II

Bones, Hypophosphatasia

Bones, Robinow Syndrome

Bones, Robinow Syndrome

Bones, Robinow Syndrome

Bones, Robinow Syndrome

Bones, Robinow Syndrome

Bones, Robinow Syndrome

Bones, Robinow Syndrome

Skin, Steatocystoma

Liver, Alagille syndrome, CK7 stain

Liver, Alagille syndrome, CD10 stain

Liver, Alagille syndrome, H&E stain

Heart, Leigh syndrome

Vulva, angiomyxoma

Vulva, angiomyxoma

Soft palate, superficial myxoma

Eyebrow, superficial myxoma

Breast, superficial myxoma

Skeletal Muscle, McArdle disease

Bone Marrow, Gaucher’s disease

Brain, Alzheimer’s disease with presenilin 1 mutation

Lung, surfactant dysfunction disorder

Uterus, MLH1-deficient endometrioid carcinoma, MLH1 stain

Peripheral nerve, Amyloidosis

Eye, Granular corneal dystrophy

Ovotestis, Simpson-Golabi-Behmel Syndrome, specimen photograph

Ovotestis, Simpson-Golabi-Behmel Syndrome, H&E stain

Ovotestis, Simpson-Golabi-Behmel Syndrome, androgen receptor

Ovotestis, Simpson-Golabi-Behmel Syndrome, inhibin stain

Ovotestis, Simpson-Golabi-Behmel Syndrome, calretinin stain

Ovotestis, Simpson-Golabi-Behmel Syndrome, PLAP stain

Brain, tuberous sclerosis

Brain, Lissencephaly Type 2

Skin, Darier disease

Placenta, non‐molar trisomy

Subscribe to Genetic Disorders